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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221708Generated: November 1, 2026

Water → HCID 23076341, compound

https://huagongshe.com/reaction/2221708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant3-(methoxymethoxy)-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 23076513—
ReactantHCID 86605756HCID 86605756—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23076341HCID 2307634157%

Reaction Steps

To a solution of tert-butyl 4-{4-[(diethoxyphosphoryl)methyl]-5-methyl-1,3-thiazol-2-yl}piperazine-1-carboxylate (2.0 g) in tetrahydrofuran (50 mL) was added sodium hydride (60% in oil, 0.20 g) at room temperature, and the mixture was stirred for 30 min. 3-(Methoxymethoxy)-1-phenyl-1H-pyrazole-4-carbaldehyde (1.1 g) was added to the reaction mixture, and the mixture was heated under reflux for 4 hrs. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography and eluted with ethyl acetate-hexane (5:95-25:75, v/v) to give tert-butyl 4-(4-{(E)-2-[3-(methoxymethoxy)-1-phenyl-1H-pyrazol-4-yl]ethenyl}-5-methyl-1,3-thiazol-2-yl)piperazine-1-carboxylate as a yellow oil (1.3 g, yield 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-c31590bf419f49cca199bdd8dad64521
Source noteuspto-grants-2008_05